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Oxalic Acid → 2,3-Dihydroxy-naphth[2,3-F]quinoxaline-7,12-dione

HRID 2093357
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인쇄 미리보기

반응식

HRID 2093357 반응식
[NH2:1][C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7](=[O:17])[C:6]=2[CH:5]=[CH:4][C:3]=1[NH2:18].[C:19](O)(=[O:23])[C:20](O)=[O:21].S(=O)(=O)(O)O>CN(C)C=O>[NH:1]1[C:2]2[C:15]3[C:14](=[O:16])[C:13]4[C:8]([C:7](=[O:17])[C:6]=3[CH:5]=[CH:4][C:3]=2[NH:18][C:20](=[O:21])[C:19]1=[O:23])=[CH:9][CH:10]=[CH:11][CH:12]=4
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 971Oxalic AcidHCID 1118Sulfuric AcidHCID 156521,2-Diaminoanthraquinone

생성물 1

HCID 442512912,3-Dihydroxy-naphth[2,3-F]quinoxaline-7,12-dione

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

1,2-Diaminoanthraquinone (1.19 g, 5 mmol) is dissolved in N,N-dimethylformamide (30 mL), and oxalic acid (0.46 g, 5 mmol) and concentrated sulfuric acid (0.1 mL) is added thereinto. After reverse flow for 16 hours, the reacted mixture is transferred into icy water (200 mL) for precipitation. The precipitate is collected and washed by hot alcohol and, so as to obtain the black compound 26, and the production rate is 30%.

후처리

  1. customthe reacted mixture is transferred into icy water (200 mL) for precipitation
  2. customThe precipitate is collected
  3. washwashed by hot alcohol

출처 및 근거

ORD 기록
ord-f3a139ed37144deeb40f96b6f4485f60
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08445492B2

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